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Research: A Case of Split Notochord Syndrome with Left Congenital Diaphragmatic Hernia: A Rare Association.

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Research: A Case of Split Notochord Syndrome with Left Congenital Diaphragmatic Hernia: A Rare Association.

J Pediatr Neurosci. 2020 Jan-Mar;15(1):42-44. doi: 10.4103/JPN.JPN_85_19. Epub 2020 Mar 18.

A Case of Split Notochord Syndrome with Left Congenital Diaphragmatic Hernia: A Rare Association.

Pan P1. https://pmlegacy.ncbi.nlm.nih.gov/pubmed/32435306

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Abstract

Split notochord syndrome is a rare neural tube malformation involving the brain, spinal cord, and vertebral column. In nearly half of the cases, the malformation also involves the gastrointestinal tract in the form of a dorsal neurenteric fistula and imperforate anus. In the literature, less than 50 cases have been reported. To the best of my knowledge, this is the first reported case associated with a left congenital diaphragmatic hernia.

Copyright: © 2020 Journal of Pediatric Neurosciences.

KEYWORDS:

Congenital anomaly; neurenteric fistula; split notochord syndromePMID: 32435306 PMCID: PMC7227745 DOI: 10.4103/JPN.JPN_85_19Free PMC Article

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